A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538888



Internal ID18837169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23802041..23822436hg38UCSC Ensembl
Innerchr15:24047188..24067583hg19UCSC Ensembl
Innerchr15:21598281..21618676hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820396
hg1920396
hg1820396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053655
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538888
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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